| Literature DB >> 26686929 |
Siwen Niu1, Longlong Si2, Dong Liu2, Andrew Zhou2, Ziwei Zhang2, Zongze Shao3, Shaomeng Wang4, Lihe Zhang2, Demin Zhou5, Wenhan Lin6.
Abstract
A new class of phenolic lactones with trivial names of spiromastilactones A-M (1-13) was isolated from a deep-sea derived Spiromastix sp. fungus. Their structures featured by various chlorination at aromatic rings were determined on the basis of extensive spectroscopic analyses. An antiviral assay revealed that most of the tested compounds exert inhibitory activity against WSN influenza virus with low cytotoxicity, while the structure-activity relationships were discussed. Spiromastilactone D (4), a 5'-chloro-2'-methoxy substituted analogue, displayed the most potent to inhibit a panel of influenza A and B viruses in addition to drug-resistant clinical isolates. Mechanistic investigation resulted in that compound 4 bonded to hemagglutinin protein (HA), potentially at the spherical head, and disrupted the HA-sialic acid receptor interaction, that is essential for the attachment and entry of all influenza viruses. In addition, compound 4 also showed inhibitory effect toward viral genome replication via targeting viral RNP complex. The synergistic effects of 4 on both viral entry and replication assumed it to be a promising lead for the development of a new influenza inhibitor.Entities:
Keywords: Antiviral effect; Influenza virus; Marine-derived fungus; Mechanistic investigation; Spiromastilactones; Spiromastix sp.
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Year: 2015 PMID: 26686929 DOI: 10.1016/j.ejmech.2015.09.037
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514